Check all your potential CRISPR sites at once
Unintended CRISPR effects can derail your project. You need a way to quickly scan your targets of interest, so you can make sure editing occurred in all the places you wanted, and none of the places you didn’t.
Our application note, Evaluate CRISPR-Cas9 edits quickly and accurately with rhAmpSeq™ targeted sequencing, introduces you to a new high-throughput NGS method for quantifying CRISPR editing efficiency. First, we explain how rhAmpSeq technology works, then we put it into action by evaluating two distinct gRNAs.
Fill out the form, get the app note, and start doing better CRISPR today!